In today's demanding world, achieving optimal health and maintaining peak performance is more crucial than ever. Many ...

If approved, sotagliflozin would be the first oral medication for patients with T1D. The FDA is reviewing the BLA for datopotamab deruxtecan (Dato-DXd), a specifically engineered TROP2-directed ...

Looking to open a new credit card but not sure if you'll get approved? There's a simple feature that many card issuers offer for free: pre-qualification. You can submit a prequalification form ...

The FDA has approved Genentech’s inavolisib (Itovebi) in combination with the CDK4/6 inhibitor palbociclib and the oestrogen-receptor antagonist fulvestrant for endocrine-resistant, PIK3CA ...

The Food and Drug Administration approved changing the expiration date on multiple types of intravenous and sterile fluids made by Baxter International earlier this week, the company said in a ...

The FDA has approved the first abuse-deterrent, immediate-release, 10 mg opioid tablet for pain management, signing off on another dosage of Protega Pharmaceuticals’ Roxybond. The nod covers ...

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The FDA has expanded the approval for Jylamvo, an oral methotrexate solution, to include pediatric patients with acute lymphoblastic leukemia (ALL). Jylamvo was the first oral methotrexate solution ...

Rahul Sidhu does not work for, consult, own shares in or receive funding from any company or organization that would benefit from this article, and has disclosed no relevant affiliations beyond ...

Please go ahead. Thank you, Lydia. Good morning, and thank you for joining today's call to discuss the recent FDA approval of ORLYNVAH. A press release with details of the approval was issued on ...

The US Food and Drug Administration (FDA) has approved Iterum Therapeutics' new drug application (NDA) for ORLYNVAH (sulopenem etzadroxil and probenecid) to treat uncomplicated urinary tract ...

ORLYNVAH is indicated for the treatment of uUTIs in adult women. Credit: 9nong/Shutterstock. The US Food and Drug Administration (FDA) has approved Iterum Therapeutics‘ new drug application (NDA) for ...